Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: Atypical molecular phenotype

Annals of Neurology

Volumn 50, Issue 2, 2001, Pages 258-261

  Head, Mark W ^a,c   Tissingh, Gerrit ^a   Uitdehaag, Bernard M J ^a   Barkhof, Frederik ^a   Bunn, Tristan J R ^b   Ironside, James W ^a   Kamphorst, Wouter ^b   Scheltens, Philip ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^c WESTERN GENERAL HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PRION PROTEIN; VALINE;

ADULT; ARTICLE; BRAIN BIOPSY; CASE REPORT; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DIFFERENTIAL DIAGNOSIS; FEMALE; HOMOZYGOSITY; HUMAN; IMMUNOCYTOCHEMISTRY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL;

ADULT; CREUTZFELDT-JAKOB SYNDROME; FEMALE; FRONTAL LOBE; HOMOZYGOTE; HUMANS; IMMUNOHISTOCHEMISTRY; NETHERLANDS; PHENOTYPE;

EID: 0034909904     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.1100     Document Type: Article

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